miRNA Expression Profiles in Isolated Ventricular Cardiomyocytes: Insights into Doxorubicin-Induced Cardiotoxicity

被引:2
作者
Romero, Yohana Dominguez [1 ,2 ]
Ortiz, Gladis Montoya [2 ]
Herran, Susana Novoa [2 ]
Mendez, Jhon Osorio [2 ,3 ]
Grosso, Luis A. Gomez [2 ,4 ]
机构
[1] Univ Nacl Colombia, Fac Sci, Doctorate Biotechnol Program, Bogota 111321, Colombia
[2] Natl Inst Hlth, Mol Physiol Grp, Subdirect Sci & Technol Res, Direct Publ, Bogota 111321, Colombia
[3] Univ Nacl Colombia, Fac Med, Dept Physiol Sci, Master Biochem Program, Bogota 111321, Colombia
[4] Univ Nacl Colombia, Fac Med, Dept Physiol Sci, Bogota 111321, Colombia
关键词
doxorubicin; cardiotoxicity; cardioprotection; miRNAs; KATP; SIRT1; FOXO1; GSK3B; HEART-FAILURE; ELECTROPHYSIOLOGICAL CHANGES; TRANSCRIPTION FACTORS; CELL-DEATH; APOPTOSIS; CYTOSCAPE; CARDIOLIPIN; MECHANISMS; SYNTHASE; ROLES;
D O I
10.3390/ijms25105272
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Doxorubicin (DOX), widely used as a chemotherapeutic agent for various cancers, is limited in its clinical utility by its cardiotoxic effects. Despite its widespread use, the precise mechanisms underlying DOX-induced cardiotoxicity at the cellular and molecular levels remain unclear, hindering the development of preventive and early detection strategies. To characterize the cytotoxic effects of DOX on isolated ventricular cardiomyocytes, focusing on the expression of specific microRNAs (miRNAs) and their molecular targets associated with endogenous cardioprotective mechanisms such as the ATP-sensitive potassium channel (KATP), Sirtuin 1 (SIRT1), FOXO1, and GSK3 beta. We isolated Guinea pig ventricular cardiomyocytes by retrograde perfusion and enzymatic dissociation. We assessed cell morphology, Reactive Oxygen Species (ROS) levels, intracellular calcium, and mitochondrial membrane potential using light microscopy and specific probes. We determined the miRNA expression profile using small RNAseq and validated it using stem-loop qRT-PCR. We quantified mRNA levels of some predicted and validated molecular targets using qRT-PCR and analyzed protein expression using Western blot. Exposure to 10 mu M DOX resulted in cardiomyocyte shortening, increased ROS and intracellular calcium levels, mitochondrial membrane potential depolarization, and changes in specific miRNA expression. Additionally, we observed the differential expression of KATP subunits (ABCC9, KCNJ8, and KCNJ11), FOXO1, SIRT1, and GSK3 beta molecules associated with endogenous cardioprotective mechanisms. Supported by miRNA gene regulatory networks and functional enrichment analysis, these findings suggest that DOX-induced cardiotoxicity disrupts biological processes associated with cardioprotective mechanisms. Further research must clarify their specific molecular changes in DOX-induced cardiac dysfunction and investigate their diagnostic biomarkers and therapeutic potential.
引用
收藏
页数:24
相关论文
共 50 条
  • [31] The significance of the apelinergic system in doxorubicin-induced cardiotoxicity
    Matusik, Katarzyna
    Kaminska, Katarzyna
    Sobiborowicz-Sadowska, Aleksandra
    Borzuta, Hubert
    Buczma, Kasper
    Cudnoch-Jedrzejewska, Agnieszka
    HEART FAILURE REVIEWS, 2024, 29 (05) : 969 - 988
  • [32] Spironolactone Attenuates Doxorubicin-induced Cardiotoxicity in Rats
    Liu, Guangzhong
    Liu, Yongwu
    Wang, Renjun
    Hou, Tingting
    Chen, Chaoyi
    Zheng, Sijia
    Dong, Zengxiang
    CARDIOVASCULAR THERAPEUTICS, 2016, 34 (04) : 216 - 224
  • [33] Endurance Exercise Attenuates Doxorubicin-induced Cardiotoxicity
    Lee, Youngil
    Kwon, Insu
    Jang, Yongchul
    Cosio-Lima, Ludmila
    Barrington, Patricia
    MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, 2020, 52 (01) : 25 - 36
  • [34] The true colors of autophagy in doxorubicin-induced cardiotoxicity
    Xiao, Bin
    Hong, Lang
    Cai, Xinyong
    Mei, Songbo
    Zhang, Ping
    Shao, Liang
    ONCOLOGY LETTERS, 2019, 18 (03) : 2165 - 2172
  • [35] Hyperhomocysteinaemia Promotes Doxorubicin-Induced Cardiotoxicity in Mice
    Fan, Rui
    Wang, Yao
    Zhang, Jinjin
    An, Xiangbo
    Liu, Shuang
    Bai, Jie
    Li, Jiatian
    Lin, Qiuyue
    Xie, Yunpeng
    Liao, Jiawei
    Xia, Yunlong
    PHARMACEUTICALS, 2023, 16 (09)
  • [36] Oxidative stress injury in doxorubicin-induced cardiotoxicity
    Mei Songbo
    Hong Lang
    Cai Xinyong
    Xiao Bin
    Zhang Ping
    Shao Liang
    TOXICOLOGY LETTERS, 2019, 307 : 41 - 48
  • [37] Effect of fermented Cordyceps sinensis on doxorubicin-induced cardiotoxicity in rats
    Wu, Rong
    Yao, Ping-An
    Wang, Hui-Lin
    Gao, Yan
    Yu, Hai-Lun
    Wang, Lei
    Cui, Xiao-Hua
    Xu, Xu
    Gao, Jian-Ping
    MOLECULAR MEDICINE REPORTS, 2018, 18 (03) : 3229 - 3241
  • [38] Potential cardioprotective effects of Amentoflavone in doxorubicin-induced cardiotoxicity in mice
    Alherz, Fatemah A.
    El-Masry, Thanaa A.
    Negm, Walaa A.
    El-Kadem, Aya H.
    BIOMEDICINE & PHARMACOTHERAPY, 2022, 154
  • [39] New insights into doxorubicin-induced cardiotoxicity: The critical role of cellular energetics
    Tokarska-Schlattner, Malgorzata
    Zaugg, Michael
    Zuppinger, Christian
    Wallimann, Theo
    Schlattner, Uwe
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2006, 41 (03) : 389 - 405
  • [40] Gene expression profiling identifies the novel role of immunoproteasome in doxorubicin-induced cardiotoxicity
    Zhao, Wen-Jie
    Wei, Sheng-Nan
    Zeng, Xiang-Jun
    Xia, Yun-Long
    Du, Jie
    Li, Hui-Hua
    TOXICOLOGY, 2015, 333 : 76 - 88